A Novel Role of the Yeast CaaX Protease Ste24 in Chitin Synthesis

Autor(en): Meissner, Derek
Odman-Naresh, Jothini
Vogelpohl, Inga
Merzendorfer, Hans 
Stichwörter: A-FACTOR PRECURSOR; ASCOSPORE WALL; Cell Biology; CELL-WALL; ENDOPLASMIC-RETICULUM; GROWTH; MEMBRANE; PROTEINS; SACCHAROMYCES-CEREVISIAE; SYNTHASE-III ACTIVITY; TOBACCO HORNWORM
Erscheinungsdatum: 2010
Herausgeber: AMER SOC CELL BIOLOGY
Journal: MOLECULAR BIOLOGY OF THE CELL
Volumen: 21
Ausgabe: 14
Startseite: 2425
Seitenende: 2433
Zusammenfassung: 
Ste24 is a membrane-integral CaaX metalloprotease residing in the endoplasmic reticulum (ER). In yeast, the only known substrate of Ste24 is the mating factor a precursor. A global screening for protein-protein interactions indicated that Ste24 interacts with chitin synthesis deficient (Chs) 3, an enzyme required for chitin synthesis. We confirmed this interaction by yeast two-hybrid analyses and mapped the interacting cytoplasmic domains. Next, we investigated the influence of Ste24 on chitin synthesis. In sterile (ste)24 Delta mutants, we observed resistance to calcofluor white (CFW), which was also apparent when the cells expressed a catalytically inactive version of Ste24. In addition, ste24 Delta cells showed a decrease in chitin levels and Chs3-green fluorescent protein localized less frequently at the bud neck. Overexpression of STE24 resulted in hypersensitivity to CFW and a slight increase in chitin levels. The CFW phenotype of ste24 Delta cells could be rescued by its human and insect orthologues. Although Chs3 binds to Ste24, it seems not to be a substrate for this protease. Instead, our data suggest that Chs3 and Ste24 form a complex in the ER that facilitates protease action on prenylated Chs4, a known activator of Chs3 with a C-terminal CaaX motif, leading to a more efficient localization of Chs3 at the plasma membrane.
ISSN: 10591524
DOI: 10.1091/mbc.E10-01-0080

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